Molecular cytogenetics, RFLP analysis and clinical characterization of a de novo trisomy 10p case
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference12 articles.
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2. Evidence of gene dosage effect for HK1 in the red cells of a patient with trisomy 10pter–pl3;Dallapiccola;Ann. Génét.,1981
3. Brother and sister with trisomy 10p: 46,XY,(22p+)mat; 46,XX, (22p+)mat;de Chieri;Hum. Genet.,1978
4. Dinucleotide repeat polymorphisms at the DI0S183 and Dl0S245 loci;Decker;Hum. Mol. Genet.,1992
5. Duplication l0p in a girl due to a maternal translocation t(10;14) (pl l;pl2);Gonzalez;Am. J. Med. Genet.,1983
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2. An unusual de novo duplication 10p/deletion 10q syndrome: The first case in Korea;Journal of Genetic Medicine;2015-06-30
3. Relatives with Opposite Chromosome Constitutions, rec(10)dup(10p)inv(10)(p15.1q26.12) and rec(10)dup(10q)inv(10)(p15.1q26.12), due to a Familial Pericentric Inversion;Cytogenetic and Genome Research;2014
4. Clinical Findings Associated with a De Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis;Case Reports in Genetics;2011
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